Zebrafish as a model of mammalian cardiac function: Optically mapping the interplay of temperature and rate on voltage and calcium dynamics
Por:
Rayani, K, Lin, E, Craig, C, Lamothe, M, Shafaattalab, S, Gunawan, M, Li, AY, Hove-Madsen, L, Tibbits, GF
Publicada:
1 oct 2018
Resumen:
The zebrafish (Danio rerio) heart is a viable model of mammalian cardiovascular function due to similarities in heart rate, ultrastructure, and action potential morphology. Zebrafish are able to tolerate a wide range of naturally occurring temperatures through altering chronotropic and inotropic properties of the heart. Optical mapping of cannulated zebrafish hearts can be used to assess the effect of temperature on excitation-contraction (EC) coupling and to explore the mechanisms underlying voltage (V-m) and calcium (Ca2+) transients.
Applicability of zebrafish as a model of mammalian cardiac physiology should be understood in the context of numerous subtle differences in structure, ion channel expression, and Ca2+ handling. In contrast to mammalian systems, Ca2+ release from the sarcoplasmic reticulum (SR) plays a relatively small role in activating the contractile apparatus in teleosts, which may contribute to differences in restitution. The contractile function of the zebrafish heart is closely tied to extracellular Ca2+ which enters cardiomyocytes through L-type Ca2+ channel (LTCC), T-type Ca2+ channel (ITCC), and the sodium calcium exchanger (NCX).
Novel data found that despite large temperature effects on heart rate, V-m, and Ca2+ durations, the relationship between V-m and Ca2+ signals was only minimally altered in the face of acute temperature change. This suggests that zebrafish V-m and Ca2+ kinetics are largely rate-independent. In comparison to mammalian systems, zebrafish Ca2+ cycling is inherently more dependent on transsarcolemmal Ca2+ transport and less reliant on SR Ca2+ release. However, the compensatory actions of various components of the Ca2+ cycling machinery of the zebrafish cardiomyocytes, allow for maintenance of EC coupling over a wide range of environmental temperatures. (C) 2018 Elsevier Ltd. All rights reserved.
Filiaciones:
Rayani, K:
Simon Fraser Univ, Dept Biomed Physiol & Kinesiol, Mol Cardiac Physiol Grp, Vancouver, BC, Canada
Lin, E:
Simon Fraser Univ, Dept Biomed Physiol & Kinesiol, Mol Cardiac Physiol Grp, Vancouver, BC, Canada
British Columbia Childrens Hosp, Dept Cardiovasc Sci, Vancouver, BC, Canada
Craig, C:
Simon Fraser Univ, Dept Biomed Physiol & Kinesiol, Mol Cardiac Physiol Grp, Vancouver, BC, Canada
Lamothe, M:
Simon Fraser Univ, Dept Biomed Physiol & Kinesiol, Mol Cardiac Physiol Grp, Vancouver, BC, Canada
Shafaattalab, S:
Simon Fraser Univ, Dept Biomed Physiol & Kinesiol, Mol Cardiac Physiol Grp, Vancouver, BC, Canada
Gunawan, M:
Simon Fraser Univ, Dept Biomed Physiol & Kinesiol, Mol Cardiac Physiol Grp, Vancouver, BC, Canada
Li, AY:
Simon Fraser Univ, Dept Biomed Physiol & Kinesiol, Mol Cardiac Physiol Grp, Vancouver, BC, Canada
Hove-Madsen, L:
Hosp Santa Creu & Sant Pau, Cardiovasc Res Ctr CSIC ICCC, Barcelona, Spain
Tibbits, GF:
Simon Fraser Univ, Dept Biomed Physiol & Kinesiol, Mol Cardiac Physiol Grp, Vancouver, BC, Canada
British Columbia Childrens Hosp, Dept Cardiovasc Sci, Vancouver, BC, Canada
Green Submitted
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